HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromo-1-methyl-2-oxoindoline → HCID 86700270, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromo-1-methyl-2-oxoindoline | HCID 2432666 | — |
| Reactant | HCID 86700271 | HCID 86700271 | — |
| Product | HCID 86700270 | HCID 86700270 | — |
Reaction Steps
(S)-2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(2-(1-methyl-2-oxoindolin-5-yl)pyridin-4-yl)benzo[d]thiazol-6-yl)acetic acid was prepared using in a similar manner as (S)-2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(2-(1-methyl-2-oxoindolin-4-yl)pyridin-4-yl)benzo[d]thiazol-6-yl)acetic acid, except 5-bromo-1-methylindolin-2-one was used instead of 4-bromo-1-methylindolin-2-one. LCMS-ESI+: calc'd for C34H31ClN3O4S: 612.1 (M+H+); Found: 612.2 (M+H+). 1H NMR (400 MHz, CD3OD) δ: 8.61 (d, 1H), 8.36 (s, 1H), 7.94 (d, 1H), 7.89 (m, 1H), 7.84 (m, 2H), 7.61-7.59 (m, 1H), 7.54-7.50 (m, 3H), 7.03 (d, 1H), 5.18 (s, 1H), 3.55 (s, 2H), 3.14 (s, 3H), 2.53 (s, 3H), 0.89 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08987250B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-bfbf37d3d19f41ee8bfd03875e5a58ac |
| Source note | uspto-grants-2015_03 |